Medical Device Recalls
-
|
1 result found
510(K) Number: K012549 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Product is a 15x16x27" (WxDxH) air purifier device with one of two different brands next to the cont... | 2 | 01/31/2012 |
FEI # 1000634072 Healthway Home Products, Inc. |
-







